Добірка наукової літератури з теми "Hydride Transfer Chemistry"
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Статті в журналах з теми "Hydride Transfer Chemistry"
McSkimming, Alex, Jordan W. Taylor, and W. Hill Harman. "Assembly and Redox-Rich Hydride Chemistry of an Asymmetric Mo2S2 Platform." Molecules 25, no. 13 (July 7, 2020): 3090. http://dx.doi.org/10.3390/molecules25133090.
Повний текст джерелаFukuzumi, Shunichi, Toshiaki Kitano, Masashi Ishikawa, and Yoshiharu Matsuda. "Electron transfer chemistry of hydride and carbanion donors. Hydride and carbanion transfer via electron transfer." Chemical Physics 176, no. 2-3 (October 1993): 337–47. http://dx.doi.org/10.1016/0301-0104(93)80244-4.
Повний текст джерелаChan, Bun, and Masanari Kimura. "High-level quantum chemistry exploration of reduction by group-13 hydrides: insights into the rational design of bio-mimic CO2 reduction." Electronic Structure 4, no. 4 (November 7, 2022): 044001. http://dx.doi.org/10.1088/2516-1075/ac9bb3.
Повний текст джерелаBohra, Anupama, Pradeep K. Sharma, and Kalyan K. Banerji. "Kinetics and Mechanism of the Oxidation of Aliphatic Aldehydes by Benzyltrimethylammonium Chlorobromate." Journal of Chemical Research 23, no. 5 (May 1999): 308–9. http://dx.doi.org/10.1177/174751989902300506.
Повний текст джерелаZhao, Yin, Helmut W. Schmalle, Thomas Fox, Olivier Blacque, and Heinz Berke. "Hydride transfer reactivity of tetrakis(trimethylphosphine)(hydrido)(nitrosyl)molybdenum(0)." Dalton Trans., no. 1 (2006): 73–85. http://dx.doi.org/10.1039/b511797f.
Повний текст джерелаWel, Hans van der, Nico M. M. Nibbering, and Margaret M. Kayser. "A gas phase study of the regioselective BH4− reduction of some 2-substituted maleic anhydrides." Canadian Journal of Chemistry 66, no. 10 (October 1, 1988): 2587–94. http://dx.doi.org/10.1139/v88-406.
Повний текст джерелаZaman, Khan M., Norio Nishimura, Shunzo Yamamoto, and Yoshimi Sueishi. "Hydride transfer reactions of Michler's hydride with different ?-accetors." Journal of Physical Organic Chemistry 7, no. 6 (June 1994): 309–15. http://dx.doi.org/10.1002/poc.610070607.
Повний текст джерелаFUKUZUMI, SHUNICHI, and SOUTA NOURA. "Cobalt(III) Porphyrin-catalysed Hydride Reduction of 10-Methylacridinium ion and Hydrometallation of Alkenes and Alkynes by Tributyltin Hydride." Journal of Porphyrins and Phthalocyanines 01, no. 03 (July 1997): 251–58. http://dx.doi.org/10.1002/(sici)1099-1409(199707)1:3<251::aid-jpp24>3.0.co;2-p.
Повний текст джерелаTassano, Erika, and Mélanie Hall. "Enzymatic self-sufficient hydride transfer processes." Chemical Society Reviews 48, no. 23 (2019): 5596–615. http://dx.doi.org/10.1039/c8cs00903a.
Повний текст джерелаCasey, Charles P., and Jeffrey B. Johnson. "Kinetic isotope effect evidence for the concerted transfer of hydride and proton from hydroxycyclopentadienyl ruthenium hydride in solvents of different polarities and hydrogen bonding ability." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1339–46. http://dx.doi.org/10.1139/v05-140.
Повний текст джерелаДисертації з теми "Hydride Transfer Chemistry"
Razzaghi, Mortezaali. "Quantum Tunneling in Hydride Transfer Reactions in Solution." Thesis, Southern Illinois University at Edwardsville, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=1549836.
Повний текст джерелаThe secondary kinetic isotope effects for the hydride transfer reactions from aliphatic alcohols to four carbocations (NAD+ models) in acetonitrile were determined. The results suggest that the hydride transfer takes place by tunneling and that the rehybridizations of both donor and acceptor carbons lag behind the H-tunneling. This is quite contrary to the observations in alcohol dehydrogenases where the importance of enzyme motions in catalysis is manifested.
Wilson, Gleason. "Hydrogen Transfer Reaction Involving Nickel POCOP-Pincer Hydride Complexes." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447688935.
Повний текст джерелаMa, Li. "Study of the Primary Isotope Dependence of Secondary Kinetic Isotope Effects in Hydride Transfer Reactions in Solution." Thesis, Southern Illinois University at Edwardsville, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10843728.
Повний текст джерелаIt has been accepted that hydrogen-transfer reactions take place through a quantum mechanical tunneling mechanism, where H tunnels through its classical energy barrier in light of its wave form. There are several H-tunneling models proposed, including the contemporary Marcus-like H-tunneling model, which explains that the donor-acceptor distance (DAD) in the tunneling ready state (TRS) is shorter for a heavier isotope (e.g. deuterium (D)) then a lighter isotope (e.g., protium (H)). This model has been used to explain the kinetic isotopic effect observations in H-tunneling processes to provide mechanistic role of protein in enzyme catalysis. The purpose of the research is to test the hypothesis of “isotopically different DAD” concept by studying the hydrogen/deuterium-transfer reactions in solutions, given that hydride-transfer reactions account for over 50% of biological reactions. Our group’s previous results showed that the steric hindrance and hydrogen-bonding effect played a significant role in the different hydrogen vs deuterium tunneling-ready states. In general, the shorter DAD creates more spatial crowding effect which will affect the 2° C-H vibrations and decrease the 2° KIEs. In this thesis, different reaction systems were designed to test these effects by studying the 1° isotope dependence of 2° KIEs at the near and remote positions from the reaction center. It was found that the results are consistent with the hypothesis of the “isotopically different TRS structures”.
Gurevic, Ilya. "Studies on the hydride transfer and other aspects of several thymidylate synthase variants." Diss., University of Iowa, 2018. https://ir.uiowa.edu/etd/6586.
Повний текст джерелаQuaye, Osbourne. "On the Preorganization of the Active Site of Choline Oxidase for Hydride Transfer and Tunneling Mechanism." Digital Archive @ GSU, 2009. http://digitalarchive.gsu.edu/chemistry_diss/46.
Повний текст джерелаDzierlenga, Michael W., and Michael W. Dzierlenga. "The Dynamics of Enzymatic Reactions: A Tale of Two Dehydrogenases." Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/620868.
Повний текст джерелаRinard, Chauncey J. "I. An Unusual Hydride Transfer in the Thermolysis of a Lithium Alkoxide ; II. Carbon-Carbon Bond Forming Reactions of Oxidized Anilide Intermediates. A New Route to Dihydroindoles /." The Ohio State University, 1996. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487935125878439.
Повний текст джерелаYuan, Hongling. "Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/56.
Повний текст джерелаBorghese, Sophie. "Toward green processes organic synthesis by catalysis with metal-doped solids." Phd thesis, Université de Strasbourg, 2013. http://tel.archives-ouvertes.fr/tel-01017796.
Повний текст джерелаBorghèse, Sophie. "Toward green processes organic synthesis by catalysis with metal-doped solids." Thesis, Strasbourg, 2013. http://www.theses.fr/2013STRAF008/document.
Повний текст джерелаNowadays, the modern chemical industry has to deal with increasing environmental concerns, including the disposal of waste and its economic impact, or the diminution of important worldwide resources such as transition metals. In this Ph.D. thesis, we aimed to bring improvement in this area by the development of green processes, based on the use of recyclable heterogeneous catalysts. By combining the catalytic properties of several metal cations with the properties of solid catalysts such as polyoxometalates or zeolites, we were able to set up new tools for organic synthesis. Silver-doped polyoxometalates proved to be very efficient catalysts in the rearrangement of alkynyloxiranes to furans. Acetals and spiroketals were synthetized by dihydroalkoxylation of alkynediols under catalysis with silver-zeolites. As a perspective, we highlighted the potential applications of such green procedures in the total synthesis of more complex molecules. The first results suggested that these environmental friendly processes should gain increasing interest in the future
Частини книг з теми "Hydride Transfer Chemistry"
Fukuzumi, Shunichi. "Proton-Coupled Electron Transfer in Hydrogen and Hydride Transfer Reactions." In Physical Inorganic Chemistry, 39–74. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470602577.ch2.
Повний текст джерелаLaw, D. W., C. Gunasekara, and S. Setunge. "Use of Brown Coal Ash as a Replacement of Cement in Concrete Masonry Bricks." In Lecture Notes in Civil Engineering, 23–25. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-3330-3_4.
Повний текст джерела"Proton Transfer, Hydrogen Atom Transfer, and Hydride Transfer." In The Proton: Applications to Organic Chemistry, 146–84. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-670370-2.50008-6.
Повний текст джерелаEpstein, Lina M., Natalia V. Belkova, and Elena S. Shubina. "Dihydrogen Bonded Complexes and Proton Transfer to Hydride Ligands by Spectral (IR, NMR) Studies." In Recent Advances in Hydride Chemistry, 391–418. Elsevier, 2001. http://dx.doi.org/10.1016/b978-044450733-4/50014-0.
Повний текст джерела"Vitamin Chemistry Drives Human Metabolic Logic." In The Chemical Biology of Human Vitamins, 414–31. The Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/bk9781788014649-00414.
Повний текст джерела"Glucose Chemical Biology." In The Chemical Biology of Carbon, 481–506. The Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781839169502-00481.
Повний текст джерелаTaber, Douglass. "Best Synthetic Methods: Oxidation and Reduction." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0003.
Повний текст джерелаWatt, C. Ian F. "Hydride Shifts and Transfers." In Advances in Physical Organic Chemistry, 57–112. Elsevier, 1988. http://dx.doi.org/10.1016/s0065-3160(08)60158-6.
Повний текст джерелаLambert, Tristan H. "New Methods for C–N Ring Construction." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0055.
Повний текст джерела"Heterocycles in Chemical Biology: II. Vitamins." In The Chemical Biology of Carbon, 306–54. The Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781839169502-00306.
Повний текст джерелаТези доповідей конференцій з теми "Hydride Transfer Chemistry"
Shen, T. C. "Nanofabrication on Silicon Surfaces by STM." In Chemistry and Physics of Small-Scale Structures. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/cps.1997.cma.1.
Повний текст джерелаJorgensen, Scott. "Engineering Hydrogen Storage Systems." In ASME 2007 2nd Energy Nanotechnology International Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/enic2007-45026.
Повний текст джерелаChen, Kok Hao, and Jong Hyun Choi. "DNA Oligonucleotide-Templated Nanocrystals: Synthesis and Novel Label-Free Protein Detection." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11958.
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